Issues Concerning Informed Consent and Protections of Human Subjects in Research

8. When participation by an individual in a research protocol is
completed, participants and/or their families are entitled to be informed
of results as soon as this information is available, to have the
opportunity to receive feedback concerning their individual
participation in the protocol, to critique the protocol, and to provide
input concerning possible additional research.
9. All participants in research protocols involving the assessment of new
medications will be provided with opportunities by the investigator for
a trial on the medication being studied, so long as other research on
the new medication has demonstrated potential safety and efficacy.
10. All individuals who have benefitted from the administration of
experimental medications in research will be provided continual access
to the medication by the investigator without cost until a source of
third party payment is found.